Class II · Moderate risk
Guaifenesin Grape liquid 100 mg/5 mL
Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.
FDA Drug Recalls
1,103 recalls, newest first
Class I · High risk
Magnesium Sulfate in Water for Injection
Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the wrong barcode which scans in as heparin sodium.
Class II · Moderate risk
Bromfenac Ophthalmic Solution 0.09%
Lack of Assurance of Sterility: Failed preservative effectiveness test